510(k) K070330 ยท FDF Colonoscope And Accessories, Flexible/Rigid
THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM
| Applicant | Avantis Medical Systems, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Apr 24, 2007 |
| Received | Feb 5, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070330
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.